WO1999003673A1 - Film wvtr avec cire incorporee a une couche adhesive perforee - Google Patents

Film wvtr avec cire incorporee a une couche adhesive perforee Download PDF

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Publication number
WO1999003673A1
WO1999003673A1 PCT/US1998/013773 US9813773W WO9903673A1 WO 1999003673 A1 WO1999003673 A1 WO 1999003673A1 US 9813773 W US9813773 W US 9813773W WO 9903673 A1 WO9903673 A1 WO 9903673A1
Authority
WO
WIPO (PCT)
Prior art keywords
layer
wax
film
intermediate layer
polyolefin
Prior art date
Application number
PCT/US1998/013773
Other languages
English (en)
Inventor
Michael Thomas Heffelfinger
Original Assignee
Mobil Oil Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mobil Oil Corporation filed Critical Mobil Oil Corporation
Priority to EP98934235A priority Critical patent/EP0996535A4/fr
Priority to BR9810724A priority patent/BR9810724A/pt
Priority to CA 2294512 priority patent/CA2294512A1/fr
Priority to JP2000502935A priority patent/JP2001510105A/ja
Priority to AU83804/98A priority patent/AU747712B2/en
Priority to KR1020007000339A priority patent/KR20010021776A/ko
Publication of WO1999003673A1 publication Critical patent/WO1999003673A1/fr

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07—Flat, e.g. panels
    • B29C48/08—Flat, e.g. panels flexible, e.g. films
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
    • B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
    • B29C55/023—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets using multilayered plates or sheets
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
    • B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04—Polymers of ethylene
    • B29K2023/08—Copolymers of ethylene
    • B29K2023/086—EVOH, i.e. ethylene vinyl alcohol copolymer
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2091/00—Use of waxes as moulding material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/24—All layers being polymeric
    • B32B2250/242—All polymers belonging to those covered by group B32B27/32
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/724—Permeability to gases, adsorption
    • B32B2307/7242—Non-permeable
    • B32B2307/7244—Oxygen barrier
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2323/00—Polyalkenes
    • B32B2323/10—Polypropylene
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2391/00—Waxes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00—Containers; Receptacles
    • B32B2439/70—Food packaging
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00—Stock material or miscellaneous articles
    • Y10S428/91—Product with molecular orientation
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/249921—Web or sheet containing structurally defined element or component
    • Y10T428/249994—Composite having a component wherein a constituent is liquid or is contained within preformed walls [e.g., impregnant-filled, previously void containing component, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31801—Of wax or waxy material
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31855—Of addition polymer from unsaturated monomers
    • Y10T428/31909—Next to second addition polymer from unsaturated monomers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31855—Of addition polymer from unsaturated monomers
    • Y10T428/31909—Next to second addition polymer from unsaturated monomers
    • Y10T428/31913—Monoolefin polymer

Definitions

  • the present invention relates to multilayer packaging films having enhanced barrier characteristics, and which are particularly useful as packaging films for food products, and are successful in laminating, printing or coating operations.
  • Plastic materials such as polymeric films have been widely used for packaging various food and non-food products. In order to insure proper preservation of products packaged in such polymeric films, it is necessary to provide the films with barriers against transmission of air, moisture, deleterious flavors, etc. No single unmodified polymeric film, however, has sufficient gas and moisture barrier characteristics needed for proper packaging requirements.
  • polyolefin films such as polypropylene films are particularly preferred in the manufacture of packaging films due to their low cost and ease of manufacture.
  • Such polypropylene films however, inherently permit the transmission of oxygen and water vapor from the outside of the film to the inside of the package made up of the film. When such films are used as food packagings, oxygen and water vapor transmitted therethrough promote rapid deterioration of foods packaged therein.
  • multilayer polymeric films have been developed having improved water vapor transmission rates (WVTR).
  • WVTR water vapor transmission rates
  • incorporating wax into film structures has been known to improve water vapor transmission rates. It is believed that the wax migrates or blooms to the outside surface of the film structure and becomes crystalline, thus imparting superior WVTR and improved oxygen barrier properties.
  • the wax on the surface is susceptible to removal, thereby presenting difficulty in maintaining such WTVR and oxygen barrier properties, particularly when such films are used in laminating, printing and coating operations.
  • U.S. Patent Nos. 5,141,801 and 5,155,160 disclose incorporating a wax into a polyolefin surface layer of a co- extruded film.
  • these patents suggest incorporating a barrier layer of polymeric material such as a polyamide or an ethylene vinyl alcohol copolymer (EVOH).
  • EVOH ethylene vinyl alcohol copolymer
  • Such polyamide and EVOH barrier layers are expensive and difficult to manufacture.
  • the prior art discloses various useful films, such films are typically susceptible to removal of the wax during subsequent laminating, printing and coating processes, and are difficult and expensive to manufacture.
  • a multilayer film having a polyolefin core layer, a copolymer or terpolymer intermediate layer on at least one surface of the polyolefin core layer, with the intermediate layer having voids therein and including a wax trapped within the voids, and a surface layer on the intermediate layer.
  • the polyolefin core layer and the surface layers are polypropylene.
  • the intermediate layer is preferably an ethylene/propylene copolymer or an ethylene/butylene/ propylene terpolymer, containing 2% to 20% of a crystalline Fischer Tropsch wax trapped within the voids therein.
  • the film is a five layer biaxially oriented film having a polypropylene core layer, cavitated or voided copolymer or terpolymer intermediate layers on both surfaces of the core layer including a wax trapped within the voids thereof, and a polypropylene surface layer on both of the intermediate layers.
  • the present invention also provides for a method of preparing such a multilayer film, which method involves co-extruding a first polyolefin resin incorporating a wax therein, a second polyolefin resin of a copolymer or terpolymer having particles dispersed therein, and a third polyolefin resin to form a multilayer base film having a polyolefin core layer including the wax, a copolymer or terpolymer intermediate layer incorporating the particles therein on at least one surface of the polyolefin core layer and a polyolefin surface layer on the intermediate layer.
  • the method further involves orienting the multilayer base film at conditions sufficient to cause the microparticles to form voids in the intermediate layer and to cause the wax to migrate from the polyolefin core layer into the voids of the intermediate layer.
  • the present invention is directed to a multilayer film structure incorporating a polyolefin core layer, a copolymer or terpolymer intermediate layer having voids therein and including a wax trapped within the voids on at least one surface of the polyolefin core layer, and a surface layer on the intermediate layer.
  • the film structure of the present invention provides excellent WVTR and oxygen barrier properties, while permitting laminating, printing and coating of the film structure without deleterious effects on the WVTR and oxygen barrier properties.
  • the polyolefin core layer contemplated by the present invention can be any suitable polyolefin polymer useful in the manufacture of thermoplastic films.
  • Particularly preferred polyolefin polymers include propylene homopolymers and copolymers.
  • Propylene homopolymers of particular use include 80 to 100% isotactic polypropylene, most preferably 95 to 96% isotactic polypropylene.
  • the propylene homopolymers have a melt index ranging from 2 to 10 grams/10 minutes and most preferably a melt index of from 3.5 to 6 grams/10 minutes.
  • Preferred propylene copolymers include 98-96/2-4 propylene/ethylene copolymers, 50/50 propylene/butene-1 copolymer, 95/5 propylene/ 1-pentene copolymer, 90/10 propylene/ 1-hexene copolymer, 80/20 propylene/4-methyl-l-pentene copolymer, etc.
  • the film structure further includes an intermediate layer or "tie" layer on at least one surface of the core layer, with the intermediate layer being a polyolefin copolymer or terpolymer.
  • the intermediate layer is provided on both surfaces of the core layer.
  • suitable polyolefin copolymers or terpolymers include without limitation ethylene- propylene (EP) copolymer and ethylene-propylene-butene-1 (EPB) terpolymer.
  • EP ethylene-propylene
  • EPB ethylene-propylene-butene-1
  • the ratio of ethylene to propylene with an ethylene-propylene copolymer is preferably 2 to 4% by weight ethylene and from 96% to 98% by weight polypropylene, while the ratio of ethylene to propylene to butene-1 for ethylene-propylene-butene-1 terpolymer is preferably from 0 to 15% ethylene, 70 to 100% propylene and 0 to 15% butene-1.
  • the intermediate layer includes voids therein, commonly referred to as "cavitations", thus providing a voided or cavitated film layer.
  • voids therein, commonly referred to as "cavitations"
  • Incorporating voided or cavitated layers into multilayer film structures is known in the art, for instance, as described in U.S. Patent No. 4,377,616.
  • voids are formed by incorporating void-initiating particals or particulate material into the resin which forms the film layer.
  • the film layer is formed including the particulate material dispersed throughout the layer.
  • the dispersed particulate material causes a strata of voids to form at the location of the particulate material, as will be discussed in more detail herein.
  • Such voids typically impart a high degree of opacity to the film.
  • the void-initiating particles can be any material which is capable of forming voids in the intermediate layer without causing degradation to the film material, such as those materials described in U.S. Patent No. 4,337,616.
  • the void-initiating particals are thermoplastic resins with a higher melting point than the polymer of the intermediate layer. Examples of preferred materials include polyamides, nylons, polyesters, acrylic resins, etc.
  • the void-initiating material is polybutylene terephthalate (PBT).
  • PBT polybutylene terephthalate
  • the PBT is incorporated into the resin which forms the intermediate layer, as will be discussed in more detail herein, in an amount of 4 to 15%, most preferably 6 to 10%.
  • a crystalline wax is incorported into the multilayer film.
  • the wax migrates into the voids in the intermediate layer, where it is concentrated.
  • the wax imparts superior WVTR and improved oxygen barrier properties to the film.
  • the wax is preferably a hydrocarbon wax, such as a mineral wax or a synthetic wax. More preferably, the wax is a polyethylene or polypropylene wax.
  • Particularly preferred waxes are polypropylene waxes prepared according to the Fischer-Tropsch process, commonly referred to as Fischer Tropsch waxes, typicallly having an average molecular weight of 640 and a melting point of 80° C.
  • the wax is initially incorporated into the core layer, and migrates into the voids of the intermediate layer during preparation and orientation of the film, as will be discussed in more detail herein.
  • all of the wax easily migrates or blooms to the surface, where it is subject to removal by wiping or subsequent processing of the film.
  • the voids in the intermediate layer provide an internal surface area to contain or trap the wax within the film structure, thus preventing all of the wax from blooming to the surface of the film.
  • the amount of wax incorporated into the film structure depends on the thickness of the overall film structure as well as the type of polyolefin layers.
  • the wax is preferably present in an amount of 2% to 20%, more preferably from 6% to 12%, and most preferably 12%. Amounts in excess of 20% tend to produce film structures which are weak.
  • the intermediate layer is a cavitated or voided polyolefin copolymer or te ⁇ olymer. It is believed that a unique synergy exists between the trapped wax and the copolymer or te ⁇ olymer voided intermediate layer. This synergy is believed to be due to the enhanced solubility of the wax in the copolymer or te ⁇ olymer and the high diffusion rate of the wax in this layer. This permits the wax to diffuse to the internal surface of the voids, creating a high density layer at the void walls.
  • the film structure of the present invention further includes a surface layer or "skin" layer on the intermediate layer.
  • a surface layer or "skin" layer on the intermediate layer.
  • surface layers are preferably provided on both of said intermediate layers.
  • the surface layer is a polyolefin layer.
  • Useful polyolefins contemplated by the present invention include any suitable polyolefin polymer useful in the manufacture of thermoplastic films.
  • Preferred polyolefin polymers include high density polyethylene, propylene homopolymers and copolymers, such as those described above as being useful as the core layer, as well as te ⁇ olymers.
  • the surface layer adjacent the intermediate layer be one of a higher melt index polyolefin, such as polypropylene homopolymer having a melt index of from 7 to 10 grams/ 10 minutes.
  • a higher melt index polyolefin such as polypropylene homopolymer having a melt index of from 7 to 10 grams/ 10 minutes.
  • the surface layer includes a propylene copolymer or te ⁇ olymer.
  • the voided intermediate layer is believed to contain a majority of the wax within the voids of the intermediate layer, thereby maintaining the barrier properties of the film structure.
  • the films of the present invention are preferably 0.5 to 1.25 mils in thickness, with the core layer preferably representing 52 to 88 percent of the total thickness, the intermediate layers preferably representing 2 to 12 percent per side of the total thickness, and the surface layers preferably representing 4 to 12 percent per side of the total thickness.
  • the film of the present invention can be clear or opaque.
  • the film is opaque, with such opacity attributed to the cavitated nature of the intermediate layer.
  • the moisture barrier or water vapor barrier of the present inventive film is below a transmission rate of 0.25 grams per 100 square inches per day, at conditions of 37.8°C (100°F) temperature and ambient relative humidity, and most preferably below a transmission rate of 0.2 grams per 100 square inches per day.
  • the multilayer film structure of the present invention is preferably a coextruded film wherein different resins form specific layers of the film structure.
  • the present invention also relates to a method of producing a multilayer oriented film structure having excellent barrier properties against the transmission of oxygen and water vapor.
  • three polyolefin resins are co-extruded to provided a multilayer base film structure having film layers corresponding to the polyolefin resins.
  • the first polyolefin resin is a core layer-forming resin which provides for the polyolefin core layer which, as noted above, is preferably a propylene homopolymer or copolymer.
  • the crystalline wax is blended or inco ⁇ orated into the core layer- forming polyolefin resin.
  • the second polyolefin resin is an intermediate layer-forming resin which provides for the intermediate layer.
  • the intermediate layer is a polyolefin copolymer or te ⁇ olymer having voids therein.
  • the intermediate layer-forming resin includes void-initiating particals or particulate material inco ⁇ orated therein.
  • the third polyolefin resin is a surface layer-forming resin which provides for the polyolefin surface layer or skin layer, preferably a propylene homopolymer, copolymer or te ⁇ olymer.
  • the three polyolefin resins are coextruded to form a multilayer base film structure having a core layer inco ⁇ orating a wax therein, an intermediate layer inco ⁇ orating void- initiating particles therein on at least one surface of the core layer, and a surface layer on the intermediate layer.
  • the three polyolefin resins are coextruded to form a five layer base film structure having a core layer inco ⁇ orating a wax therein, an intermediate layer inco ⁇ orating void-initiating particles therein on both surfaces of the core layer, and surface layers on both intermediate layers.
  • the multilayer base film structure thus formed represents a transitional or interim product, which is then subjected to orientation to produce a multilayer oriented film product.
  • Orientation of such extruded base films is well known in the art, and results in improved physical properties of the composite layers such as flex-cracking resistance, Elmendorff tear strength, elongation, tensile strength, impact strength and cold strength properties.
  • orientation of the multilayer base film structure provides for both cavitation of the intermediate layer as well as migration of the wax into the cavitations or voids.
  • orientation of the multilayer base film structure is conducted at orientation conditions such that the void-initiating particles in the intermediate layer create voids within the structure of the intermediate layer, as described in the inco ⁇ orated U.S. Patent No. 4,377,616.
  • the film is biaxially oriented 4 to 6 times in the machine direction and 7 to 12 times in the transverse direction, more preferably 4 to 5 times in the machine direction and 8 to 10 times in the transverse direction.
  • orientation of the multilayer base film structure is conducted at conditions which cause the wax inco ⁇ orated into the core layer to become mobile, thereby causing the wax to flow or migrate.
  • orientation of the film is conducted at a temperature of 100° C to 160°C.
  • the intermediate layer is present on the surface of the wax-containing core layer, and the orientation of the film causes the voids to form within the intermediate layer as well as causes the wax within the core layer to become fluid and mobile within the film structure, the mobile wax migrates from the core layer into the voids created within the intermediate layer. As the oriented film cools, the mobile wax crystallizes within the voids of the intermediate layer, where it is in effect "trapped" within the multilayer film structure. Thus, the wax is prevented from migrating entirely to the surface of the film. It is contemplated that a portion of the wax remains within the core layer of the film structure.
  • Films manufactured according to the present invention have excellent WVTR and oxygen barrier properties, which properties are less susceptible to damage by removal of the wax from the surface as compared with prior art films. As such, the films of the present invention are useful in subsequent laminating, printing and coating techniques while retaining their WVTR and oxygen barrier properties.
  • Example 1 This example (comparative) demonstrates the effects of inco ⁇ orating wax into the core of a five layer film structure having a polypropylene homopolymer core layer, polypropylene homopolymer intermediate layers on each surface of the core layer, and polypropylene homopolymer surface layers on each of the intermediate layers.
  • a polypropylene homopolymer resin was blended with 4.5% of a Fischer Tropsch wax having a melting point of 80° C.
  • This polypropylene/wax resin blend was co-extruded with two additional polypropylene homopolymer resins, to form a five layer base film structure having a polypropylene homopolymer core layer inco ⁇ orating 4.5% wax therein, polypropylene homopolymer intermediate layers on both surfaces of the core layer, and polypropylene homopolymer surface layers on both of the intermediate layers.
  • the five layer base film structure was biaxially oriented 4 to 5 times in the machine direction and 8 to 10 times in the transverse direction, to produce a clear five layer film product.
  • the five layer film product was aged in a hot room at 48.9°C (120°F) and ambient humidity for a period of 72 hours, and tested for water vapor transmission according to ASTM method F124-90 and oxygen transmission according to ASTM method D3985-81.
  • the five layer film had a poor water vapor transmission rate of 0.30 g/ 100 in 2 /day, and a poor oxygen transmission of 70 cc/100 in 2 /day.
  • This example (comparative) demonstrates the effects of inco ⁇ orating wax into the core of a three layer film structure having a polypropylene homopolymer core and including non- cavitated te ⁇ olymer surface layers.
  • a polypropylene homopolymer resin was blended with 4.5% of a Fischer Tropsch wax having a melting point of 80° C as in Example 1.
  • This propylene/wax resin blend was coextruded with a te ⁇ olymer resin including an ethylene/butylene/propylene te ⁇ olymer, to form a three layer base film intermediate structure having a polypropylene homopolymer core layer inco ⁇ orating 4.5% wax therein, ethylene/butalene/propylene te ⁇ olymer surface layers on both of the intermediate layers.
  • the three layer base film intermediate structure was biaxially oriented 4 to 5 times in the machine direction and 8 to 10 times in the transverse direction, to produce a clear three layer film product.
  • the three layer film product was aged in a hot room at 48.9°C (120°F) and ambient humidity for a period of 72 hours, and tested for water vapor transmission according to ASTM method F124-90 and oxygen transmission according to ASTM method D3985-81.
  • the three layer film had an excellent water vapor transmission rate of 0.08 g/100 in 2 / day, and a good oxygen transmission of 37.3 cc/100 in 2 /day. Most of the wax, however, bloomed to the surface of the film, and was vulnerable to wiping, thereby increasing the water vapor transmission and oxygen transmission, and decreasing the barrier properties.
  • This example represents a comparative example wherein the intermediate layer is a cavitated polypropylene homopolymer rather than a cavitated copolymer or te ⁇ olymer, and demonstrates the effects of inco ⁇ orating wax into the core of a five layer film structure having a polypropylene homopolymer core layer, a cavitated polypropylene homopolymer intermediate layer on both surfaces of the core layer, and a polypropylene homopolymer surface layer on each of the intermediate layers.
  • a polypropylene homopolymer resin was blended with 4.5% of a Fischer Tropsch wax having a melting point of 80° C.
  • a second polypropylene homopolymer was blended with 6% polybutylene terephthalate (PBT) as a void-initiating material.
  • PBT polybutylene terephthalate
  • These two resin blends were co- extruded with a third polypropylene homopolymer resin, to form a five layer base film intermediate structure having a polypropylene homopolymer core layer inco ⁇ orating 4.5% wax therein, polypropylene homopolymer intermediate layers inco ⁇ orating 6% PBT on both surfaces of the core layer, and polypropylene homopolymer surface layers on both of the intermediate layers.
  • the five layer base film intermediate structure was biaxially oriented 4 to 5 times in the machine direction and 8 to 10 times in the transverse direction.
  • the orientation of the film produced voids in the intermediate layer, and caused the wax in the core layer to become mobile and migrate into the voids in the intermediate layer wherein it crystallized.
  • an opaque five layer film product having a cavitated or voided intermediate layer including a wax trapped within the voids.
  • the five layer film product was aged in a hot room at 48.9°C (120°F) and ambient humidity for a period of 72 hours, and tested for water vapor transmission according to ASTM method F124-90 and oxygen transmission according to ASTM method D3985-81.
  • the five layer film had a poor water vapor transmission rate of 0.35 g/100 in 2 /day, and a poor oxygen transmission of 112.1 cc/100 in 2 /day. Examples 4 & 5
  • Examples 4 and 5 represent films manufactured according to the present invention, thus demonstrating the effects of inco ⁇ orating wax into the core of a five layer film structure having a polypropylene homopolymer core layer, a cavitated ethyelene/propylene copolymer or ethylene/butylene/propylene te ⁇ olymer intermediate layer on both surfaces of the core layer, and a polypropylene homopolymer surface layer on each of the intermediate layers.
  • Example 4 a polypropylene homopolymer resin was blended with 4.5% of a Fischer Tropsch wax having a melting point of 80° C. An ethylene/propylene copolymer was blended with 6% polybutylene terephthalate (PBT) as a void-initiating material. These two resin blends were co-extruded with a third polypropylene homopolymer resin, to form a five layer base film intermediate structure having a polypropylene homopolymer core layer inco ⁇ orating 4.5% wax therein, ethylene/propylene copolymer intermediate layers inco ⁇ orating 6% PBT on both surfaces of the core layer, and polypropylene homopolymer surface layers on both of the intermediate layers.
  • PBT polybutylene terephthalate
  • the five layer base film intermediate structure was biaxially oriented 4 to 5 times in the machine direction and 8 to 10 times in the transverse direction.
  • the orientation of the film produced voids in the intermediate layer, and caused the wax in the core layer to become mobile and migrate into the voids in the intermediate layer wherein it crystallized.
  • an opaque five layer film product having a cavitated or voided intermediate layer including a wax trapped within the voids was formed.
  • Example 5 a film was prepared as in Example 4, with the exception that an ethylene/butylene/propylene te ⁇ olymer was substituted for the ethylene/propylene copolymer of the intermediate layers.
  • the five layer film of Example 4 had a good water vapor transmission rate of 0.22 g/100 in 2 /day, and a good oxygen transmission of 69.1 cc/100 in 2 /day.
  • the five layer film of Example 5 had a good water vapor transmission rate of 0.20 g/100 in 2 /day, and a good oxygen transmission of 62.6 cc/100 in 2 /day.
  • a comparison of Examples 4 and 5 with Example 1 demonstrates the improved barrier to water vapor transmission and oxygen transmission by inco ⁇ orating a cavitated intermediate layer into the film structure.
  • a comparison of Examples 4 and 5 with Example 2 demonstrates the importance of a cavitated intermediate layer, in that the film of Example 2 possessed excellent barrier properties, but the wax was easily susceptible to romoval by wiping of the surface.
  • a comparison of Examples 4 and 5 with Example 3 demonstrates the benefits of using a cavitated copolymer or te ⁇ olymer as the intermediate layer as compared with a cavitated homopolymer as the intermediate layer, with improved WVTR and oxygen permeability properties achieved with the cavitated copolyer or te ⁇ olymer intermediate layers. Examples 6-11
  • Examples 6-11 demonstrate the improved water vapor transmission rate and oxygen barrier properties obtained by inco ⁇ orating increased amounts of wax into the core of a five layer film structure having a polypropylene homopolymer core layer, a cavitated ethylene/propylene copolymer or ethylene/butylene/propylene te ⁇ olymer intermediate layer on both surfaces of the core layer, and a polypropylene homopolymer surface layer on each of the intermediate layers, as in the present invention.
  • polypropylene homopolymer resins were blended with 6%, 9% and 12%, respectively, of a Fischer Tropsch wax having a melting point of 80° C.
  • An ethylene/propylene copolymer was blended with 10% polybutylene terephthalate (PBT) as a void-initiating material.
  • PBT polybutylene terephthalate
  • the polypropylene homopolymer/wax resins were individually coextruded with the ethylene/propylene copolymer and a third polypropylene homopolymer resin having a melt index of 9 grams/ 10 minutes, to form three (3) separate five layer base film intermediate structures having a polypropylene homopolymer core layer inco ⁇ orating, respectively, 6%, 9% and 12% wax therein, ethylene/propylene copolymer intermediate layers inco ⁇ orating 10% PBT on both surfaces of the core layer, and polypropylene homopolymer surface layers on both of the intermediate layers.
  • Each of the five layer base film intermediate structures were biaxially oriented 4 to 5 times in the machine direction and 8 to 10 times in the transverse direction.
  • the orientation of the films produced voids in the intermediate layers, and caused the wax in the core layers to become mobile and migrate into the voids in the intermediate layers wherein it crystallized.
  • three opaque five layer film products having cavitated or voided intermediate layers including a wax trapped within the voids were formed.
  • Example 9 three films were prepared as in Example 6, 7 and 8, with the exception that an ethylene/butylene/propylene te ⁇ olymer was substituted for the ethylene/propylene copolymer of the intermediate layers.
  • three opaque five layer film products having cavitated or voided intermediate layers of ethylene/butylene/propylene te ⁇ olymer including a wax trapped within the voids were formed.
  • the five layer film products of Examples 6-11 were aged in a hot room at 48.9°C (120°F) and ambient humidity for a period of 72 hours, and tested for water vapor transmission according to ASTM method F 124-90 and oxygen transmission according to ASTM method D3985-81. The results of the tests are shown in Table A.
  • each of the five layer films of Examples 6-11 had excellent water vapor transmission rates and oxygen transmission rates. Furthermore, a comparison of Examples 6, 7 and 8, representing increased levels of wax with a cavitated copolymer intermediate layer, as well as a comparison of Examples 9, 10 and 11, representing increased levels of wax with a cavitated te ⁇ olymer intermediate layer, demonstrate that improved water vapor transmission and oxygen barrier properties are achieved with increased levels of wax. Furthermore, the water vapor transmission rate remains at an acceptable level after wiping of the surface of the film, suggesting that the wax is trapped within the voids of the intermediate layer.

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)

Abstract

L'invention concerne un film multicouches présentant des propriétés de protection améliorées, notamment contre la pénétration de vapeur d'oxygène et d'eau. Ce film multicouches est constitué: d'une couche centrale de polyoléfine; d'une couche intermédiaire de copolymère ou de terpolymère, placée sur au moins l'une des surfaces de ladite couche centrale de polyoléfine, cette couche intermédiaire présentant des vides dans lesquels une cire a été insérée; et d'une couche superficielle, placée sur ladite couche intermédiaire. Les films multicouches fabriqués selon la présente invention sont particulièrement utiles en tant que films d'emballage pour des produits alimentaires, et dans des opérations de stratification, d'impression, ou d'enduisage.
PCT/US1998/013773 1997-07-16 1998-07-01 Film wvtr avec cire incorporee a une couche adhesive perforee WO1999003673A1 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP98934235A EP0996535A4 (fr) 1997-07-16 1998-07-01 Film wvtr avec cire incorporee a une couche adhesive perforee
BR9810724A BR9810724A (pt) 1997-07-16 1998-07-01 Pelìcula com proporção de transmissão de vapor d'água melhorada usando cera em combinação com uma camada de amarração cavitada
CA 2294512 CA2294512A1 (fr) 1997-07-16 1998-07-01 Film wvtr avec cire incorporee a une couche adhesive perforee
JP2000502935A JP2001510105A (ja) 1997-07-16 1998-07-01 空洞化された結合層と組み合わせた、ワックスを使用した、改善された水蒸気透過率のフィルム
AU83804/98A AU747712B2 (en) 1997-07-16 1998-07-01 Improved WVTR film using wax in combination with a cavitated tie layer
KR1020007000339A KR20010021776A (ko) 1997-07-16 1998-07-01 공동화된 결속층과 왁스를 병합 사용하여 수증기 투과율을개선시킨 필름

Applications Claiming Priority (2)

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US08/895,510 1997-07-16
US08/895,510 US6033771A (en) 1997-07-16 1997-07-16 WVTR film using wax in combination with a cavitated tie layer

Publications (1)

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WO1999003673A1 true WO1999003673A1 (fr) 1999-01-28

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EP (1) EP0996535A4 (fr)
JP (1) JP2001510105A (fr)
KR (1) KR20010021776A (fr)
CN (1) CN1265062A (fr)
AR (1) AR016346A1 (fr)
AU (1) AU747712B2 (fr)
BR (1) BR9810724A (fr)
CA (1) CA2294512A1 (fr)
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WO (1) WO1999003673A1 (fr)

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US8957148B2 (en) 2013-01-29 2015-02-17 Chevron Phillips Chemical Company Lp Polymer compositions having improved barrier properties
US9676920B2 (en) 2007-11-27 2017-06-13 Basell Poliolefine Italia S.R.L. Polyolefin nanocomposites materials

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US7695822B2 (en) * 2005-05-10 2010-04-13 Toray Plastics (America), Inc. Tie-layer for polyolefin films
US20070031653A1 (en) * 2005-08-02 2007-02-08 Toray Plastics (America), Inc. Multi-layer barrier film structure
US7666518B2 (en) * 2006-07-12 2010-02-23 Toray Plastics (America), Inc. Reprocessed polyhydroxy amino ether coated polypropylene film
US20080205800A1 (en) * 2007-02-28 2008-08-28 Toray Plastics (America), Inc. Transparent biaxially oriented polypropylene film with low moisture vapor and oxygen transmission rate
EP2193025B1 (fr) * 2007-09-25 2011-02-23 ExxonMobil Chemical Patents Inc. Films opaques blancs présentant des propriétés élastiques et des propriétés de barrière améliorées
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WO2015006856A1 (fr) 2013-07-19 2015-01-22 Marcel Riendeau Élément d'échangeur de chaleur/enthalpique et procédé de fabrication associé
US9630383B2 (en) 2014-05-20 2017-04-25 Toray Plastics (America), Inc. Biaxially oriented polypropylene film with low moisture vapor transmission rate
BR112018000507B1 (pt) 2015-07-10 2023-01-24 Berry Global, Inc Processo para a fabricação de um filme respirável microporoso
US20170015821A1 (en) 2015-07-13 2017-01-19 Toray Plastics (America), Inc. Transparent oriented polypropylene film with high moisture vapor and oxygen barrier properties
CN108778674B (zh) * 2015-11-05 2022-02-11 贝瑞全球有限公司 聚合物膜和用于制造聚合物膜的方法
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WO2000009329A1 (fr) * 1998-08-13 2000-02-24 Hoechst Trespaphan Gmbh Feuille de polypropylene multicouche a orientation biaxiale, presentant des proprietes barriere ameliorees, son procede de production et son utilisation
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US9676920B2 (en) 2007-11-27 2017-06-13 Basell Poliolefine Italia S.R.L. Polyolefin nanocomposites materials
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US8957148B2 (en) 2013-01-29 2015-02-17 Chevron Phillips Chemical Company Lp Polymer compositions having improved barrier properties

Also Published As

Publication number Publication date
ID25614A (id) 2000-10-19
KR20010021776A (ko) 2001-03-15
EP0996535A1 (fr) 2000-05-03
BR9810724A (pt) 2000-08-08
AR016346A1 (es) 2001-07-04
CN1265062A (zh) 2000-08-30
EP0996535A4 (fr) 2002-06-05
AU747712B2 (en) 2002-05-23
US6033771A (en) 2000-03-07
JP2001510105A (ja) 2001-07-31
CA2294512A1 (fr) 1999-01-28
AU8380498A (en) 1999-02-10

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